首页> 外文期刊>Frontiers in Veterinary Science >Evaluation of Duration of Immunogenicity and Protective Efficacy of Improved Influenza Viral Vector–Based Brucella abortus Vaccine Against Brucella melitensis Infection in Sheep and Goats
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Evaluation of Duration of Immunogenicity and Protective Efficacy of Improved Influenza Viral Vector–Based Brucella abortus Vaccine Against Brucella melitensis Infection in Sheep and Goats

机译:基于流感病毒载体为基础的羊毛菌免受Brucella melitensis感染的改良流感病毒载体的胸腺菌持续时间和保护效果的评价

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In this study, we first evaluated the duration of a protective immune response against B. melitensis infection in non-pregnant sheep and goats immunized with an improved (by vaccine formulation and route of administration) commercial B. abortus vaccine based on influenza viral vectors expressing Brucella immunodominant Omp16, L7/L12, Omp19 or Cu-Zn SOD proteins (Flu-BA_Omp19-SOD). Sheep and goats in the vaccinated group were immunized thrice concurrently via the subcutaneous and conjunctival routes of administration at an interval of 21 days. Animals in the control group were administered with 20% Montanide Gel01 adjuvant in PBS in the same way. We showed that Flu-BA_Omp19-SOD vaccine in sheep and goats induces antigen-specific Th1 biased (IgG2a over IgG1) antibody response and T-cell and IFN-γ responses lasting over a period of one month post-last vaccination (PLV). The levels of protection against B. melitensis 16M infection (vaccination efficacy) in vaccinated sheep for a period of six months was 0-20% and in goats 20-40% compared to control challenge group. But the severity of B. melitensis 16M infection in Flu-BA_Omp19-SOD vaccinated sheep and goats during the entire period of observation revealed the infection index (P=0.001-P0.0001) and Brucella colonization in lymph nodes and organs (P=0.04-P0.0001) was significantly lower than control group. To conclude, Flu-BA_Omp19-SOD vaccine using improved formulation and administration method in sheep and goats provides augmented antigen specific humoral and T-cell immune response lasting only for 1 month PLV, and partial protection for 6 months against B. melitensis 16M infection.
机译:在这项研究中,我们首先评估了在非孕妇绵羊和山羊免疫(通过疫苗制剂和给药途径)的山羊在非孕妇绵羊和山羊中进行了保护性免疫反应的持续时间。基于表达流感病毒载体的商业B. abortus疫苗Brucella免疫肿瘤OMP16,L7 / L12,OMP19或Cu-Zn SOD蛋白(流感-Ba_POP19-SOD)。疫苗接种组中的绵羊和山羊通过皮下和结膜给药途径在21天的间隔中同时免疫接种。对照组中的动物以相同的方式用20%蒙土凝胶01佐剂施用。我们展示了绵羊和山羊的流感 - Ba_omp19-SOD疫苗诱导抗原特异性Th1偏置(IgG2a通过IgG1)抗体反应和T细胞和IFN-γ反应在最后一次接种后的一个月内持续到持续的时间(PLV)。与对照攻击组相比,疫苗绵羊疫苗绵羊中的疫苗接种绵羊(疫苗接种功效)的保护水平为六个月,山羊20%,而达20%。但B.Melitensis 16M感染在整个观察期间流感Ba_omp19-SOD接种疫苗绵羊和山羊的严重程度揭示了淋巴结和器官中的感染指数(P = 0.001-P <0.0001)和Brucella殖民化(P = 0.04 -P <0.0001)显着低于对照组。为了得出结论,使用改进的配方和羊羊和山羊的流感Ba_omp19-SOD疫苗提供增强的抗原特异性体液和T细胞免疫反应,仅持续1个月PLV,并偏离B.Melitensis 16M感染6个月。

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